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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772632Generated: November 2, 2026

N-bromobutanimide → Ethyl 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylate

https://huagongshe.com/reaction/1772632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylateHCID 14207617—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylateHCID 117727933—

Reaction Steps

To a solution of compound 1c (3.2 g, 9.0 mmol) in DCM (100 mL) at 0° C. was added NBS (1.6 g, 9.0 mmol) portionwise. The reaction mixture was allowed to stir at rt for 10 min, and subsequently was washed with a saturated aqueous sodium bicarbonate (2×100 mL). The organic layer was separated, dried over Na2SO4 and concentrated under reduced pressure to give compound 21a as an off-white solid. Mass Spectrum (LCMS, ESI pos.) Calcd. For C13H15BrN4O3: 356.2 (M+H). Found 356.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-cde9cdc915ac4fc3828daca598e78800
Source noteuspto-grants-2016_02